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MEMO1 Antibody (C-16): sc-83725

 |  Datasheet

(Based on data analysis)
  • MEMO1 Antibody (C-16) is a rabbit polyclonal IgG provided at 100 µg/ml
  • epitope mapping near the C-terminus of MEMO1 of human origin
  • recommended for detection of MEMO1 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, porcine and avian
  • blocking peptide, sc-83725 P
 

See additional MEMO Antibodies including MEMO and MEMO1.

Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IF   siRNA  
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
MEMO1 Antibody (C-16) sc-83725 100 µg/ml $279
MEMO1 (C-16) P sc-83725 P
(peptide)
 100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
MEMO1 siRNA (h) sc-106215 10 µM $258
MEMO1 siRNA (m) sc-149368 10 µM $258
MEMO1 (h)-PR sc-106215-PR 10 µM, 20 µl $23
MEMO1 (m)-PR sc-149368-PR 10 µM, 20 µl $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
MEMO1 shRNA Plasmid (h) sc-106215-SH 20 µg $520
MEMO1 shRNA Plasmid (m) sc-149368-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
MEMO1 shRNA (h) Lentiviral Particles sc-106215-V 200 µl $625
MEMO1 shRNA (m) Lentiviral Particles sc-149368-V 200 µl $625
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAdd 
SK-MEL-28 Cell Lysate sc-2236 500 µg/200 µl $104
A-375 Cell Lysate sc-3811 500 µg/200 µl $104

MEMO1 (mediator of cell motility 1), also known as C2orf4 or NS5ATP7, is a 297 amino acid protein that is thought to relax extracellular chemotactic signals that are targeted at the microtubule cytoskeleton, thereby controlling cell migration. Additionally, MEMO1 is thought to mediate Neu signaling and is required for breast carcinoma migration, suggesting an important role in tumorigenesis. The gene encoding MEMO1 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the chromosome 2-localized ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes, which also map to chromosome 2.